Ochsenreither Sebastian, Kuhls Katrin, Schaar Matthias, Presber Wolfgang, Schönian Gabriele
Institute of Microbiology and Hygiene, Charité Universitätsmedizin Berlin, Dorotheenstr. 96, 10117 Berlin, Germany.
J Clin Microbiol. 2006 Feb;44(2):495-503. doi: 10.1128/JCM.44.2.495-503.2006.
The Leishmania donovani complex, which consists of L. donovani, L. infantum-L. chagasi, and L. archibaldi, is responsible for visceral manifestations of leishmaniasis. Multilocus enzyme electrophoresis is the standard method for the characterization and identification of strains of Leishmania. For L. infantum, the predominance of zymodeme MON-1 significantly reduces the discriminative power of this approach. In the present study, we developed 17 independent polymorphic microsatellite markers for the typing of strains of L. infantum, with the main emphasis on zymodeme MON-1. The discriminative powers of 11 markers selected from among these markers were tested by using a panel of 63 isolates of the L. donovani complex. Unique multilocus genotypes were observed for the strains analyzed, with only three exceptions. Model-based and distance-based analyses of the data set showed comparable results. It was possible to discriminate between L. donovani sensu stricto, a non-MON-1 group of L. infantum isolates, and a MON-1 group of L. infantum isolates. Within MON-1, three clusters with geographical correlations became apparent. The frequency of heterozygosity in the alleles analyzed varied extremely between the different groups of isolates. The main clusters described are not consistent with species definitions based on isoenzyme analysis but confirm the results of former PCR-based investigations.
杜氏利什曼原虫复合体由杜氏利什曼原虫、婴儿利什曼原虫-恰加斯利什曼原虫和阿奇巴尔德利什曼原虫组成,可引发利什曼病的内脏表现。多位点酶电泳是用于利什曼原虫菌株鉴定和特征描述的标准方法。对于婴儿利什曼原虫,酶带型MON-1占主导显著降低了该方法的鉴别能力。在本研究中,我们开发了17个独立的多态性微卫星标记用于婴儿利什曼原虫菌株分型,主要针对酶带型MON-1。从这些标记中选取的11个标记的鉴别能力通过使用一组63株杜氏利什曼原虫复合体分离株进行了测试。在所分析的菌株中观察到了独特的多位点基因型,仅有三个例外。基于模型和基于距离的数据集分析显示了可比的结果。可以区分狭义杜氏利什曼原虫、婴儿利什曼原虫分离株的非MON-1组以及婴儿利什曼原虫分离株的MON-1组。在MON-1内,出现了三个与地理相关的聚类。所分析等位基因中的杂合频率在不同分离株组之间差异极大。所描述的主要聚类与基于同工酶分析的物种定义不一致,但证实了以前基于PCR研究的结果。
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